Canonical Allele Identifier: PA2830209296
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1041275
ClinVar RCV Id: RCV001345056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32832Ser
CA349406649
NM_133378.4:c.98495C>G
CA349406656
NM_133378.4:c.98494A>T